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Massive national database launched to crack the code on rare inherited colon diseases

NCT ID NCT07461246

Summary

This study is creating a large national registry in Italy to collect information on patients with inherited conditions that cause many polyps in the colon, which can lead to cancer. It aims to understand how these diseases progress, see how well current monitoring and surgical treatments work in real life, and find ways to improve care standards across the country. The study is observational, meaning it collects data from patients' medical records and ongoing care but does not test a new treatment.

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Fondazione IRCCS Istituto Nazionale dei Tumori

    Milan, 20133, Italy

Conditions

Explore the condition pages connected to this study.